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Results: 1 to 20 of 34 (representing 18 labs)

Tests names and labsConditionsGenes and analytesMethods

Werner syndrome

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Melanoma Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
911
  • C Sequence analysis of the entire coding region

WRN. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Werner Syndrome via the WRN Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Chromosomal Instability Syndromes Sequencing Panel

PreventionGenetics
United States
108
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Lipodystrophies and progeroid syndromes (NGS panel for 25 genes)

CGC Genetics
Portugal
2525
  • C Sequence analysis of the entire coding region

Progeroid syndromes (NGS panel for 12 genes)

CGC Genetics
Portugal
1212
  • C Sequence analysis of the entire coding region

Lipodystrophies and progeroid syndromes (NGS panel for 25 genes)

CGC Genetics
Portugal
2525
  • C Sequence analysis of the entire coding region

Progeroid syndromes (NGS panel for 12 genes)

CGC Genetics
Portugal
1212
  • C Sequence analysis of the entire coding region

Werner Syndrome , Sequencing WRN Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Hereditary Thyroid Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Blueprint Genetics
Finland
14116
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Pediatric Solid Tumors Panel

Invitae
United States
9148
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Werner Syndrome Test

Invitae
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sarcoma Comprehensive Panel

Fulgent Genetics
United States
92026
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cancer Panel

Fulgent Genetics
United States
1735124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Werner syndrome: WRN gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Invitae Multi-Cancer Panel

Invitae
United States
14180
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CarrierMap

Recombine
United States
300298
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Progeria syndromes Panel

CeGaT GmbH
Germany
2018
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 34

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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